Polyamic acid solution, polyimide resin and flexible metal clad laminate using the same
a technology of polyimide resin and polyimide resin, which is applied in the direction of pretreatment surfaces, plasma techniques, synthetic resin layered products, etc., can solve the problems of short circuit wiring, curling, and polyimide resin cannot exhibit its natural characteristics sufficiently, and achieve high adhesive strength
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example 1
[0058]1-1. Preparation of a Polyamic Acid Solution
[0059]Through a 4-neck reaction vessel provided with a thermometer, a stirrer, a nitrogen inlet and a powder dispensing funnel, nitrogen gas was slowly passed, while 166 ml of N-methyl pyrrolidone (NMP) and 6.8 g (20 wt %) of talc powder were added, followed by stirring. To the solution, 7.11 g (0.0657 mol) of p-phenylenediamine (p-PDA) and 3.32 g (0.0166 mol) of 4,4′-oxydianiline (ODA) were added, and the resultant mixture was completely dissolved by being stirred at 25° C. To the resultant solution, 21.77 g (0.0740 mol) of 3,3′,4,4′-biphenyltetracarboxylic acid dianhydride (BPDA) and 1.79 g (0.0082 mol) of pyromellitic dianhydride (PMDA) were slowly added, and the mixture was polymerized by being stirred for 10 hours so as to provide a polyamic acid solution having a viscosity of 25,000 cps.
[0060]1-2. Fabrication of Flexible Copper Clad Laminate
[0061]By using a casting method, the prepared polyamic acid solution was coated on the s...
example 2
[0062]By using an atmospheric plasma generator, on the surface of the polyimide layer of the flexible copper clad laminate obtained from Example 1-2, atmospheric plasma treatment was carried out.
[0063]
[0064]gas: argon gas, oxygen gas, nitrogen gas
[0065]strength of plasma: 7 kV
[0066]distance between an electrode and a polyimide layer: 5 mm
[0067]treatment speed: 1 m / min
example 3
[EXAMPLE 3] TO [EXAMPLE 8], AND [COMPARATIVE EXAMPLE 1] TO [COMPARATIVE EXAMPLE 7]
[0068]As noted in Tables 1 and 2 below, a polyamic acid solution and a flexible copper clad laminate were prepared in the same manner as described in Example 2, except that the contents of p-phenylenediamine (p-PDA), 4,4′-oxydianiline (ODA), 3,3′,4,4′-biphenyltetracarboxylic acid dianhydride (BPDA), pyromellitic dianhydride (PMDA), and talc were changed.
TABLE 1Exp 1Exp 2Exp 3Exp 4Exp 5Exp 6Exp 7Exp 8BPDAAmount (g)21.7721.7720.7520.5219.6517.5812.913.065Mol0.07400.07400.07050.06970.06680.05980.04380.044PMDAAmount (g)1.791.792.712.682.575.599.569.68Mol0.00820.00820.01240.01230.01180.02560.04380.0444PMDA / (BPDA + PMDA)0.100.100.150.150.150.300.500.50p-PDAAmount (g)7.117.117.186.664.677.387.117.68Mol0.06570.06570.06640.06160.04320.06820.06570.0710ODAAmount (g)3.323.323.364.147.113.454.423.59Mol0.01660.01660.01680.02070.03550.01720.02210.0179p-PDA / (p-PDA + ODA)0.800.800.800.750.550.800.750.80Diamine / Dianhydr...
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